HappeningToo topic
Rosuvastatin reports
Browse community reports connected to Rosuvastatin. These reports can show that other people are describing similar experiences, but they do not prove that Rosuvastatin caused a symptom or reaction.
⚕️ Medicine safety note
Community reports do not prove causation, cannot be used to estimate how common a reaction is, and are not medical advice.
45 problems
Abdominal Discomfort while using Rosuvastatin
FDA FAERS contains adverse-event reports in which Rosuvastatin and abdominal discomfort appear together. This does not establish that Rosuvastatin caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Distension while using Rosuvastatin
FDA FAERS contains adverse-event reports in which Rosuvastatin and abdominal distension appear together. This does not establish that Rosuvastatin caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain Upper while using Rosuvastatin
FDA FAERS contains adverse-event reports in which Rosuvastatin and abdominal pain upper appear together. This does not establish that Rosuvastatin caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain while using Rosuvastatin
FDA FAERS contains adverse-event reports in which Rosuvastatin and abdominal pain appear together. This does not establish that Rosuvastatin caused the reported reaction and cannot be used to estimate how often it occurs.
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Acid reflux while using Rosuvastatin
FDA FAERS contains adverse-event reports in which Rosuvastatin and acid reflux appear together. This does not establish that Rosuvastatin caused the reported reaction and cannot be used to estimate how often it occurs.
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Alopecia while using Rosuvastatin
FDA FAERS contains adverse-event reports in which Rosuvastatin and alopecia appear together. This does not establish that Rosuvastatin caused the reported reaction and cannot be used to estimate how often it occurs.
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Anxiety while using Rosuvastatin
FDA FAERS contains adverse-event reports in which Rosuvastatin and anxiety appear together. This does not establish that Rosuvastatin caused the reported reaction and cannot be used to estimate how often it occurs.
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Back Pain while using Rosuvastatin
FDA FAERS contains adverse-event reports in which Rosuvastatin and back pain appear together. This does not establish that Rosuvastatin caused the reported reaction and cannot be used to estimate how often it occurs.
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Chest Discomfort while using Rosuvastatin
FDA FAERS contains adverse-event reports in which Rosuvastatin and chest discomfort appear together. This does not establish that Rosuvastatin caused the reported reaction and cannot be used to estimate how often it occurs.
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Constipation while using Rosuvastatin
FDA FAERS contains adverse-event reports in which Rosuvastatin and constipation appear together. This does not establish that Rosuvastatin caused the reported reaction and cannot be used to estimate how often it occurs.
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Cough while using Rosuvastatin
FDA FAERS contains adverse-event reports in which Rosuvastatin and cough appear together. This does not establish that Rosuvastatin caused the reported reaction and cannot be used to estimate how often it occurs.
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Decreased Appetite while using Rosuvastatin
FDA FAERS contains adverse-event reports in which Rosuvastatin and decreased appetite appear together. This does not establish that Rosuvastatin caused the reported reaction and cannot be used to estimate how often it occurs.
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Dehydration while using Rosuvastatin
FDA FAERS contains adverse-event reports in which Rosuvastatin and dehydration appear together. This does not establish that Rosuvastatin caused the reported reaction and cannot be used to estimate how often it occurs.
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Diarrhea while using Rosuvastatin
FDA FAERS contains adverse-event reports in which Rosuvastatin and diarrhea appear together. This does not establish that Rosuvastatin caused the reported reaction and cannot be used to estimate how often it occurs.
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Dizziness while using Rosuvastatin
FDA FAERS contains adverse-event reports in which Rosuvastatin and dizziness appear together. This does not establish that Rosuvastatin caused the reported reaction and cannot be used to estimate how often it occurs.
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Dyspepsia while using Rosuvastatin
FDA FAERS contains adverse-event reports in which Rosuvastatin and dyspepsia appear together. This does not establish that Rosuvastatin caused the reported reaction and cannot be used to estimate how often it occurs.
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Excessive sweating while using Rosuvastatin
FDA FAERS contains adverse-event reports in which Rosuvastatin and excessive sweating appear together. This does not establish that Rosuvastatin caused the reported reaction and cannot be used to estimate how often it occurs.
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Fatigue while using Rosuvastatin
FDA FAERS contains adverse-event reports in which Rosuvastatin and fatigue appear together. This does not establish that Rosuvastatin caused the reported reaction and cannot be used to estimate how often it occurs.
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Feeling Abnormal while using Rosuvastatin
FDA FAERS contains adverse-event reports in which Rosuvastatin and feeling abnormal appear together. This does not establish that Rosuvastatin caused the reported reaction and cannot be used to estimate how often it occurs.
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Flushing while using Rosuvastatin
FDA FAERS contains adverse-event reports in which Rosuvastatin and flushing appear together. This does not establish that Rosuvastatin caused the reported reaction and cannot be used to estimate how often it occurs.
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Headache while using Rosuvastatin
FDA FAERS contains adverse-event reports in which Rosuvastatin and headache appear together. This does not establish that Rosuvastatin caused the reported reaction and cannot be used to estimate how often it occurs.
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Heart Rate Increased while using Rosuvastatin
FDA FAERS contains adverse-event reports in which Rosuvastatin and heart rate increased appear together. This does not establish that Rosuvastatin caused the reported reaction and cannot be used to estimate how often it occurs.
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Hives while using Rosuvastatin
FDA FAERS contains adverse-event reports in which Rosuvastatin and hives appear together. This does not establish that Rosuvastatin caused the reported reaction and cannot be used to estimate how often it occurs.
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Hypotension while using Rosuvastatin
FDA FAERS contains adverse-event reports in which Rosuvastatin and hypotension appear together. This does not establish that Rosuvastatin caused the reported reaction and cannot be used to estimate how often it occurs.
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Insomnia while using Rosuvastatin
FDA FAERS contains adverse-event reports in which Rosuvastatin and insomnia appear together. This does not establish that Rosuvastatin caused the reported reaction and cannot be used to estimate how often it occurs.
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Itching while using Rosuvastatin
FDA FAERS contains adverse-event reports in which Rosuvastatin and itching appear together. This does not establish that Rosuvastatin caused the reported reaction and cannot be used to estimate how often it occurs.
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Malaise while using Rosuvastatin
FDA FAERS contains adverse-event reports in which Rosuvastatin and malaise appear together. This does not establish that Rosuvastatin caused the reported reaction and cannot be used to estimate how often it occurs.
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Muscle Spasms while using Rosuvastatin
FDA FAERS contains adverse-event reports in which Rosuvastatin and muscle spasms appear together. This does not establish that Rosuvastatin caused the reported reaction and cannot be used to estimate how often it occurs.
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Muscular Weakness while using Rosuvastatin
FDA FAERS contains adverse-event reports in which Rosuvastatin and muscular weakness appear together. This does not establish that Rosuvastatin caused the reported reaction and cannot be used to estimate how often it occurs.
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Myalgia while using Rosuvastatin
FDA FAERS contains adverse-event reports in which Rosuvastatin and myalgia appear together. This does not establish that Rosuvastatin caused the reported reaction and cannot be used to estimate how often it occurs.
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Nausea while using Rosuvastatin
FDA FAERS contains adverse-event reports in which Rosuvastatin and nausea appear together. This does not establish that Rosuvastatin caused the reported reaction and cannot be used to estimate how often it occurs.
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Pain while using Rosuvastatin
FDA FAERS contains adverse-event reports in which Rosuvastatin and pain appear together. This does not establish that Rosuvastatin caused the reported reaction and cannot be used to estimate how often it occurs.
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Palpitations while using Rosuvastatin
FDA FAERS contains adverse-event reports in which Rosuvastatin and palpitations appear together. This does not establish that Rosuvastatin caused the reported reaction and cannot be used to estimate how often it occurs.
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Peripheral swelling while using Rosuvastatin
FDA FAERS contains adverse-event reports in which Rosuvastatin and peripheral swelling appear together. This does not establish that Rosuvastatin caused the reported reaction and cannot be used to estimate how often it occurs.
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Rash while using Rosuvastatin
FDA FAERS contains adverse-event reports in which Rosuvastatin and rash appear together. This does not establish that Rosuvastatin caused the reported reaction and cannot be used to estimate how often it occurs.
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Shortness of breath while using Rosuvastatin
FDA FAERS contains adverse-event reports in which Rosuvastatin and shortness of breath appear together. This does not establish that Rosuvastatin caused the reported reaction and cannot be used to estimate how often it occurs.
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Skin redness while using Rosuvastatin
FDA FAERS contains adverse-event reports in which Rosuvastatin and skin redness appear together. This does not establish that Rosuvastatin caused the reported reaction and cannot be used to estimate how often it occurs.
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Sleepiness while using Rosuvastatin
FDA FAERS contains adverse-event reports in which Rosuvastatin and sleepiness appear together. This does not establish that Rosuvastatin caused the reported reaction and cannot be used to estimate how often it occurs.
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Tingling or pins and needles while using Rosuvastatin
FDA FAERS contains adverse-event reports in which Rosuvastatin and tingling or pins and needles appear together. This does not establish that Rosuvastatin caused the reported reaction and cannot be used to estimate how often it occurs.
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Tremor while using Rosuvastatin
FDA FAERS contains adverse-event reports in which Rosuvastatin and tremor appear together. This does not establish that Rosuvastatin caused the reported reaction and cannot be used to estimate how often it occurs.
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Vision Blurred while using Rosuvastatin
FDA FAERS contains adverse-event reports in which Rosuvastatin and vision blurred appear together. This does not establish that Rosuvastatin caused the reported reaction and cannot be used to estimate how often it occurs.
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Vomiting while using Rosuvastatin
FDA FAERS contains adverse-event reports in which Rosuvastatin and vomiting appear together. This does not establish that Rosuvastatin caused the reported reaction and cannot be used to estimate how often it occurs.
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Weakness while using Rosuvastatin
FDA FAERS contains adverse-event reports in which Rosuvastatin and weakness appear together. This does not establish that Rosuvastatin caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Decreased while using Rosuvastatin
FDA FAERS contains adverse-event reports in which Rosuvastatin and weight decreased appear together. This does not establish that Rosuvastatin caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Increased while using Rosuvastatin
FDA FAERS contains adverse-event reports in which Rosuvastatin and weight increased appear together. This does not establish that Rosuvastatin caused the reported reaction and cannot be used to estimate how often it occurs.
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